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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276091Generated: October 26, 2026

Trifluoroacetic acid → 3-Chloro-2-(4-hydroxycarbonylmethyl-3-nitrophenyl)-5-tri-fluoromethylpyridine

https://huagongshe.com/reaction/1276091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant3-Chloro-2-[4-(bis-[1,1-dimethylethoxycarbonyl]methyl)-3-nitrophenyl]-5-trifluoromethylpyridineHCID 22114838—
SolventDichloromethaneHCID 6344—
Product3-Chloro-2-(4-hydroxycarbonylmethyl-3-nitrophenyl)-5-tri-fluoromethylpyridineHCID 22114856—

Reaction Conditions

Temperature23 °C

Reaction Steps

16 ml of trifluoroacetic acid were added dropwise to a solution of 10.2 g of 3-chloro-2-[4-(bis-[1,1-dimethylethoxycarbonyl]-methyl)-3-nitrophenyl]-5-trifluoromethylpyridine in 100 ml of anhydrous dichloromethane. After stirring at 23° C. for 65 hours, the methylene chloride was removed by distillation. The residue was dissolved in 100 ml of ether, after which the ether phase was extracted three times with 50 ml of water each time, dried over sodium sulfate and concentrated. The crude product was stirred with n-hexane/ether (9:1). Yield: 5.1 g (72%) of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06165941
Source datasetuspto-grants-2000_12
ORD IDord-dceb09d04ba74385bbb4da0d3dc8e8e2
Source noteuspto-grants-2000_12